Review of Reported Clinical Information System Adverse Events in US Food and Drug Administration Databases.
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Classifying health information technology patient safety related incidents - an approach used in WalesSafety huddles to proactively identify and address electronic health record safetyAn analysis of electronic health record-related patient safety concernsElectronic health record-related safety concerns: a cross-sectional survey.Resilient Practices in Maintaining Safety of Health Information TechnologiesUsing FDA reports to inform a classification for health information technology safety problems.Patient safety problems associated with heathcare information technology: an analysis of adverse events reported to the US Food and Drug Administration.The impact of electronic records on patient safety: a qualitative studyAdverse Events Involving Radiation Oncology Medical Devices: Comprehensive Analysis of US Food and Drug Administration Data, 1991 to 2015.Rights and responsibilities of users of electronic health records.Intelligent Simulation Model To Facilitate EHR TrainingTailoring implementation strategies for evidence-based recommendations using computerised clinical decision support systems: protocol for the development of the GUIDES tools.Measuring and improving patient safety through health information technology: The Health IT Safety Framework.Creating an oversight infrastructure for electronic health record-related patient safety hazards.Defining health information technology-related errors: new developments since to err is human.Electronic health records and national patient-safety goalsElectronic Health Record-Related Safety Concerns: A Cross-Sectional Survey of Electronic Health Record UsersExploring the sociotechnical intersection of patient safety and electronic health record implementation.Reporting medical device safety incidents to regulatory authorities: An analysis and classification of technology-induced errors.Problems with health information technology and their effects on care delivery and patient outcomes: a systematic review.An analysis of electronic health record-related patient safety incidents.Software-Related Recalls of Health Information Technology and Other Medical Devices: Implications for FDA Regulation of Digital Health.A clinical decision support tool for improving adherence to guidelines on anticoagulant therapy in patients with atrial fibrillation at risk of stroke: A cluster-randomized trial in a Swedish primary care setting (the CDS-AF study).A systematic review of trials evaluating success factors of interventions with computerised clinical decision support
P2860
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P2860
Review of Reported Clinical Information System Adverse Events in US Food and Drug Administration Databases.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Review of Reported Clinical In ...... Drug Administration Databases.
@ast
Review of Reported Clinical In ...... Drug Administration Databases.
@en
type
label
Review of Reported Clinical In ...... Drug Administration Databases.
@ast
Review of Reported Clinical In ...... Drug Administration Databases.
@en
prefLabel
Review of Reported Clinical In ...... Drug Administration Databases.
@ast
Review of Reported Clinical In ...... Drug Administration Databases.
@en
P2093
P2860
P1476
Review of Reported Clinical In ...... Drug Administration Databases.
@en
P2093
Dean F Sittig
Risa B Myers
Stephen L Jones
P2860
P356
10.4338/ACI-2010-11-RA-0064
P577
2011-01-01T00:00:00Z